Sheldon E. Cremer

679 total citations
56 papers, 488 citations indexed

About

Sheldon E. Cremer is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Sheldon E. Cremer has authored 56 papers receiving a total of 488 indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Organic Chemistry, 27 papers in Inorganic Chemistry and 6 papers in Molecular Biology. Recurrent topics in Sheldon E. Cremer's work include Organophosphorus compounds synthesis (40 papers), Phosphorus compounds and reactions (29 papers) and Synthesis and characterization of novel inorganic/organometallic compounds (20 papers). Sheldon E. Cremer is often cited by papers focused on Organophosphorus compounds synthesis (40 papers), Phosphorus compounds and reactions (29 papers) and Synthesis and characterization of novel inorganic/organometallic compounds (20 papers). Sheldon E. Cremer collaborates with scholars based in United States, Saudi Arabia and Russia. Sheldon E. Cremer's co-authors include George A. Gray, Robert J. Chorvat, Kenneth L. Marsi, R. Srinivasan, MAZHAR‐UL‐HAQUE MAZHAR‐UL‐HAQUE, Frederick L. Weitl, Dennis W. Bennett, W. Seth Horne, Phillip E. Fanwick and Donald W. Davis and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Physical Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Sheldon E. Cremer

48 papers receiving 450 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sheldon E. Cremer United States 12 427 217 49 46 26 56 488
Jacques Navech France 13 490 1.1× 268 1.2× 32 0.7× 35 0.8× 21 0.8× 52 530
Peter Bougeard Canada 14 316 0.7× 190 0.9× 72 1.5× 47 1.0× 23 0.9× 25 436
Andreas Gerold Germany 10 622 1.5× 234 1.1× 91 1.9× 43 0.9× 21 0.8× 12 685
P. Beck Germany 9 400 0.9× 252 1.2× 46 0.9× 21 0.5× 20 0.8× 11 438
Dieter Hänssgen Germany 15 443 1.0× 321 1.5× 28 0.6× 22 0.5× 19 0.7× 47 489
Raymond D. Baechler United States 12 432 1.0× 249 1.1× 63 1.3× 68 1.5× 15 0.6× 17 514
Alan E. Sopchik United States 15 480 1.1× 113 0.5× 119 2.4× 56 1.2× 39 1.5× 40 569
Michel Sanchez France 13 381 0.9× 268 1.2× 29 0.6× 19 0.4× 17 0.7× 44 429
Robert Hässig Switzerland 9 560 1.3× 181 0.8× 46 0.9× 84 1.8× 39 1.5× 10 597
Gernot Heckmann Germany 13 472 1.1× 358 1.6× 63 1.3× 20 0.4× 25 1.0× 78 619

Countries citing papers authored by Sheldon E. Cremer

Since Specialization
Citations

This map shows the geographic impact of Sheldon E. Cremer's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sheldon E. Cremer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sheldon E. Cremer more than expected).

Fields of papers citing papers by Sheldon E. Cremer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sheldon E. Cremer. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sheldon E. Cremer. The network helps show where Sheldon E. Cremer may publish in the future.

Co-authorship network of co-authors of Sheldon E. Cremer

This figure shows the co-authorship network connecting the top 25 collaborators of Sheldon E. Cremer. A scholar is included among the top collaborators of Sheldon E. Cremer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sheldon E. Cremer. Sheldon E. Cremer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Cremer, Sheldon E., et al.. (1999). Stereospecific thionation of 2-ethoxy-1,2-oxaphosphorinane 2-oxide and its derivatives with Lawesson's reagent. Canadian Journal of Chemistry. 77(7). 1274–1280. 9 indexed citations
2.
Troev, K., et al.. (1999). A new synthetic approach to?-aminophosphonic acids: Synthesis and NMR characterization. Heteroatom Chemistry. 10(7). 627–631. 7 indexed citations
3.
Cremer, Sheldon E., et al.. (1999). Stereospecific thionation of 2-ethoxy-1,2-oxaphosphorinane 2-oxide and its derivatives with Lawesson's reagent. Canadian Journal of Chemistry. 77(7). 1274–1280.
4.
Cremer, Sheldon E., et al.. (1996). PREPARATIONS AND TRANSFORMATIONS OF BIFUNCTIONAL EXO-2-PHOSPHORUS SUBSTITUTED BICYCLO[2.2.1]HEPTANES. Phosphorus, sulfur, and silicon and the related elements. 115(1). 241–254. 6 indexed citations
5.
Cremer, Sheldon E., et al.. (1996). Conformational study of six-membered phostones. cis- and trans-3-(Methoxycarbonyl)-2-methoxy-2-oxo-1,2-oxaphosphorinane. Journal of the Chemical Society Perkin Transactions 2. 2221–2221. 6 indexed citations
6.
Cremer, Sheldon E., et al.. (1995). Preparation, Reactions, and Stereochemistry of 4-tert-Butyl-1-chlorophosphorinane 1-Oxide and Derivatives. The Journal of Organic Chemistry. 60(20). 6281–6288. 11 indexed citations
7.
Bennett, Dennis W., et al.. (1992). Crystal and molecular structure of trans-(tricarbonyl)bis(trans-2,2,3,4,4-pentamethyl-1-phenylphosphetane)iron. Journal of Chemical Crystallography. 22(1). 83–90. 5 indexed citations
8.
Cremer, Sheldon E., et al.. (1990). Preparation, characterization, and reactions of 3-germabicyclo[3.2.1]octane and 2-germabicyclo[2.2.1]heptane derivatives. Organometallics. 9(6). 1784–1792. 5 indexed citations
9.
MAZHAR‐UL‐HAQUE, MAZHAR‐UL‐HAQUE, et al.. (1989). Crystal and molecular structure of phenylbenzyl-1-(2,2,3-trimethylcyclopropyl)phosphine oxide. Journal of Chemical Crystallography. 19(6). 1009–1016. 1 indexed citations
10.
Cremer, Sheldon E., et al.. (1987). Synthesis and Stereochemical Studies of Derivatives of 1,4-Dimethyl-2-phosphabicyclo[2.2.1]heptane. Phosphorous and Sulfur and the Related Elements. 30(3-4). 664–664.
11.
Shen, Quang, et al.. (1981). The molecular structures of 3-silabicyclo(3.2.1)octane and endo-3-methyl-3-silabicyclo(3.2.1)octane as determined by gas phase electron diffraction. Journal of Organometallic Chemistry. 214(2). 155–168. 2 indexed citations
12.
Horne, W. Seth, et al.. (1980). The synthesis, stereochemistry, and crystal structure of exo-3-p-nitrobenzyl-endo-3-phenyl-3-phosphoniabicyclo[3.2.1]octane bromide. Journal of the Chemical Society Perkin Transactions 2. 1467–1467. 4 indexed citations
13.
Cremer, Sheldon E., et al.. (1973). Substituted 1-chlorophosphetanium salts. Synthesis, stereochemistry, and reactions. The Journal of Organic Chemistry. 38(18). 3199–3207. 16 indexed citations
14.
Gray, George A. & Sheldon E. Cremer. (1972). 13C nuclear magnetic resonance of organophosphorus compounds: dihedral dependence of the 2 J PCC spin coupling in four-membered cyclic phosphines. Journal of the Chemical Society Chemical Communications. 367–367. 21 indexed citations
15.
Cremer, Sheldon E., et al.. (1971). Rates of Hydroxide Decomposition of Cyclic Phosphonium Salts. The Journal of Organic Chemistry. 36(21). 3226–3231. 9 indexed citations
16.
Cremer, Sheldon E.. (1970). Stereochemical assignments in phosphetane compounds. Journal of the Chemical Society D Chemical Communications. 616–616. 2 indexed citations
17.
Cremer, Sheldon E., et al.. (1969). Rates of deuterium exchange in phosphetanium salts. Journal of the Chemical Society D Chemical Communications. 1456–1456. 2 indexed citations
18.
Cremer, Sheldon E., et al.. (1968). Pyramidal inversion in substituted phosphetanes. Tetrahedron Letters. 9(55). 5799–5802. 17 indexed citations
19.
Cremer, Sheldon E.. (1968). Alkaline hydrolysis of 2,2,3,4,4-pentamethyl-1-phenylphosphetanium bromide. Chemical Communications (London). 1132–1132. 1 indexed citations
20.
Srinivasan, R. & Sheldon E. Cremer. (1965). Photochemical Rearrangement Reactions of 2-n-Propylcyclopentanone. The Journal of Physical Chemistry. 69(9). 3145–3147. 2 indexed citations

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